Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents

Detalhes bibliográficos
Autor(a) principal: Pineiro, Marta
Data de Publicação: 2001
Outros Autores: Pereira, Mariette M., Rocha Gonsalves, A. M. d'A., Arnaut, Luis G., Formosinho, Sebastião J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/5228
https://doi.org/10.1016/S1010-6030(00)00382-8
Resumo: Flash photolysis and photoacoustic calorimetry were used to measure the energy-transfer rates and singlet oxygen quantum yields originated by the triplet states of halogenated tetrakisphenylporphyrins and related chlorins in aerated toluene. The chlorins ([lambda]max[approximate]660 nm, [var epsilon][approximate]3×104 M-1 cm-1) have long-lived triplet states (>12 [mu]s) in the absence of molecular oxygen, and in its presence the singlet oxygen production quantum yields of the 2-chloro and 2,6-dichlorophenyl derivatives are 0.89±0.05 and 0.98±0.02, respectively. The high absorptivity in the red, the photostability and the efficiency of these chlorins in producing singlet oxygen suggests a ground for the development of better sensitisers for photodynamic therapy.
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spelling Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agentsPhotoacoustic calorimetryChlorinSinglet oxygenSensitisersPhotodynamic therapyFlash photolysis and photoacoustic calorimetry were used to measure the energy-transfer rates and singlet oxygen quantum yields originated by the triplet states of halogenated tetrakisphenylporphyrins and related chlorins in aerated toluene. The chlorins ([lambda]max[approximate]660 nm, [var epsilon][approximate]3×104 M-1 cm-1) have long-lived triplet states (>12 [mu]s) in the absence of molecular oxygen, and in its presence the singlet oxygen production quantum yields of the 2-chloro and 2,6-dichlorophenyl derivatives are 0.89±0.05 and 0.98±0.02, respectively. The high absorptivity in the red, the photostability and the efficiency of these chlorins in producing singlet oxygen suggests a ground for the development of better sensitisers for photodynamic therapy.http://www.sciencedirect.com/science/article/B6TGY-41YG70D-7/1/de6fc7896eaf9c58239551fa798e3e7b2001info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/5228http://hdl.handle.net/10316/5228https://doi.org/10.1016/S1010-6030(00)00382-8engJournal of Photochemistry and Photobiology A: Chemistry. 138:2 (2001) 147-157Pineiro, MartaPereira, Mariette M.Rocha Gonsalves, A. M. d'A.Arnaut, Luis G.Formosinho, Sebastião J.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-11-06T16:59:56Zoai:estudogeral.uc.pt:10316/5228Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:22.360962Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents
title Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents
spellingShingle Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents
Pineiro, Marta
Photoacoustic calorimetry
Chlorin
Singlet oxygen
Sensitisers
Photodynamic therapy
title_short Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents
title_full Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents
title_fullStr Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents
title_full_unstemmed Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents
title_sort Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents
author Pineiro, Marta
author_facet Pineiro, Marta
Pereira, Mariette M.
Rocha Gonsalves, A. M. d'A.
Arnaut, Luis G.
Formosinho, Sebastião J.
author_role author
author2 Pereira, Mariette M.
Rocha Gonsalves, A. M. d'A.
Arnaut, Luis G.
Formosinho, Sebastião J.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Pineiro, Marta
Pereira, Mariette M.
Rocha Gonsalves, A. M. d'A.
Arnaut, Luis G.
Formosinho, Sebastião J.
dc.subject.por.fl_str_mv Photoacoustic calorimetry
Chlorin
Singlet oxygen
Sensitisers
Photodynamic therapy
topic Photoacoustic calorimetry
Chlorin
Singlet oxygen
Sensitisers
Photodynamic therapy
description Flash photolysis and photoacoustic calorimetry were used to measure the energy-transfer rates and singlet oxygen quantum yields originated by the triplet states of halogenated tetrakisphenylporphyrins and related chlorins in aerated toluene. The chlorins ([lambda]max[approximate]660 nm, [var epsilon][approximate]3×104 M-1 cm-1) have long-lived triplet states (>12 [mu]s) in the absence of molecular oxygen, and in its presence the singlet oxygen production quantum yields of the 2-chloro and 2,6-dichlorophenyl derivatives are 0.89±0.05 and 0.98±0.02, respectively. The high absorptivity in the red, the photostability and the efficiency of these chlorins in producing singlet oxygen suggests a ground for the development of better sensitisers for photodynamic therapy.
publishDate 2001
dc.date.none.fl_str_mv 2001
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/5228
http://hdl.handle.net/10316/5228
https://doi.org/10.1016/S1010-6030(00)00382-8
url http://hdl.handle.net/10316/5228
https://doi.org/10.1016/S1010-6030(00)00382-8
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Photochemistry and Photobiology A: Chemistry. 138:2 (2001) 147-157
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